| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ABCC2, LOC126861013 (R1100C) | Single nucleotide variant (missense variant) | Dubin-Johnson syndrome +1 more | |
| | ABCC2, LOC126861013 (V1127I) | Single nucleotide variant (missense variant) | not provided | GConflicting classifications of pathogenicity |
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